Molecularly imprinted polymer (MIP)-coated green carbon dots-based sensing platforms
Document Type
Syllabus
Publication Date
1-1-2024
Abstract
Due to their many superiorities such as excellent optical features, chemical inertness, easy preparation, low toxicity, good solubility in aqıeous solutions, low cost and abundance of precursors, etc., carbon dots (CDs) received a gradually increasing attention in various applications areas (i.e., sensors, bioimaging, photodynamic therapy, drug delivery, etc.) On the other hand, molecularly imprinted polymers (MIPs) are artificial materials that exhibit great recognition and selectivity for the target compound/s. Because of the numerous advantages of MIPs including multiple and selective binding sites, facile preparation, robustness, great stability under extreme process conditions such as high temperature and pH values, combination of MIPs and CDs attracted high research interests to increase the sensitivity and selectivity of CDs-based sensing platforms. This chapter presents and discusses the latest developments on the design and preparation of green CDs coated with MIPs as environmentally friendly and sensitive sensor platforms for food and environmental samples. It starts with the description and superior properties of both MIPs and CDs in the introduction part. In the further sections, green aspects and synthesis approaches for CDs are described. In the last section, food and environmental applications of MIP-coated green CDs-based sensors are presented.
Identifier
85193364719 (Scopus)
ISBN
[9780443154317, 9780443154324]
Publication Title
Green Imprinted Materials: From Design to Environmental and Food Applications
External Full Text Location
https://doi.org/10.1016/B978-0-443-15431-7.00004-0
First Page
435
Last Page
452
Recommended Citation
Keçili, Rüstem; Hussain, Chaudhery Ghazanfar; and Hussain, Chaudhery Mustansar, "Molecularly imprinted polymer (MIP)-coated green carbon dots-based sensing platforms" (2024). Faculty Publications. 1013.
https://digitalcommons.njit.edu/fac_pubs/1013